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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

Venoline 140 den — Class I MDR by Inverdia AB

MD Atlas
Inverdia AB

EUDAMED last updated this device on May 18, 2026

Venoline 140 den

73310044323C

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Inverdia AB
UDI-DI code: 07331004432416
Reference / catalog number: VN432LNU

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View device family (Basic UDI)

Manufacturer information

Organization name: Inverdia AB
SRN: SE-MF-000047520
Manufacturer status: Active

Related devices

Venoline 140 den73310044323COn the market Venoline 140 den73310044323COn the market Venoline 140 den73310044323COn the market Venoline 140 den73310044323COn the market Venoline 140 den73310044323COn the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW999
Too high compression.

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Market distribution

Primary placement in Sweden; available across 1 country total.

Country	On market since	Until
SwedenPrimary placement		Still on market

Device identification

Trade name: Venoline 140 den
UDI-DI code: 07331004432416
Basic UDI-DI: 73310044323C
Reference / catalog number: VN432LNU
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Knee-long stocking with pressure 18 mm Hg at ankle and 13 mm Hg at calf. 1 pair. Size large. Colour nude (light beige).
Additional information URL: https://media.inverdia.com/2021/12/Venoline-140-den.pdf
Clinical sizes: select size from measured leg circumferences

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)07331004432416

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

M030405COMPRESSION STOCKINGS

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

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